The ACCELERATE Plus (assessment and communication excellence for safe patient outcomes) Trial Protocol: a stepped-wedge cluster randomised trial, cost-benefit analysis, and process...

por Liu, Mark, Whittam, Susan, Thornton, Anna, Goncharov, Liza, Slade, Diana, McElduff, Benjamin, Kelly, Patrick, Law, Chi Kin, Walsh, Sarah, Pollnow, Vivien, Cuffe, Jayde, McMahon, Jake, Aggar, Christina, Bilo, Jacqueline, Bowen, Karen, Chow, Josephine S. F., Duffy, Katharine, Everett, Bronwyn, Ferguson, Caleb, Frost, Steven A., Gleeson, Narelle, Hackett, Kate, Komusanac, Ivanka, Marshall, Sonia, May, Sharon, McErlean, Gemma, Melbourne, Gregory, Murphy, Jade, Newbury, Joanne, Newman, Deb, Rihari-Thomas, John, Sciuriaga, Hayley, Sturgess, Lauren, Taylor, Joanne, Tuqiri, Karen, McInnes, Elizabeth, Middleton, Sandy
Publicado 2023

Correction: the ACCELERATE Plus (assessment and communication excellence for safe patient outcomes) Trial Protocol: a stepped-wedge cluster randomised trial, cost-benefit analysis,...

por Liu, Mark, Whittam, Susan, Thornton, Anna, Goncharov, Liza, Slade, Diana, McElduff, Benjamin, Kelly, Patrick, Law, Chi Kin, Walsh, Sarah, Pollnow, Vivien, Cuffe, Jayde, McMahon, Jake, Aggar, Christina, Bilo, Jacqueline, Bowen, Karen, Chow, Josephine S. F., Duffy, Katharine, Everett, Bronwyn, Ferguson, Caleb, Frost, Steven A., Gleeson, Narelle, Hackett, Kate, Komusanac, Ivanka, Marshall, Sonia, May, Sharon, McErlean, Gemma, Melbourne, Gregory, Murphy, Jade, Newbury, Joanne, Newman, Deb, Rihari-Thomas, John, Sciuriaga, Hayley, Sturgess, Lauren, Taylor, Joanne, Tuqiri, Karen, McInnes, Elizabeth, Middleton, Sandy
Publicado 2023

Avian Influenza A(H7N2) Virus in Human Exposed to Sick Cats, New York, USA, 2016

por Marinova-Petkova, Atanaska, Laplante, Jen, Jang, Yunho, Lynch, Brian, Zanders, Natosha, Rodriguez, Marisela, Jones, Joyce, Thor, Sharmi, Hodges, Erin, De La Cruz, Juan A., Belser, Jessica, Yang, Hua, Carney, Paul, Shu, Bo, Berman, LaShondra, Stark, Thomas, Barnes, John, Havers, Fiona, Yang, Patrick, Trock, Susan C., Fry, Alicia, Gubareva, Larisa, Bresee, Joseph S., Stevens, James, Daskalakis, Demetre, Liu, Dakai, Lee, Christopher T., Torchetti, Mia Kim, Newbury, Sandra, Cigel, Francine, Toohey-Kurth, Kathy, St. George, Kirsten, Wentworth, David E., Lindstrom, Stephen, Davis, C. Todd
Publicado 2017

Diagnosis of lethal or prenatal‐onset autosomal recessive disorders by parental exome sequencing

por Stals, Karen L., Wakeling, Matthew, Baptista, Júlia, Caswell, Richard, Parrish, Andrew, Rankin, Julia, Tysoe, Carolyn, Jones, Garan, Gunning, Adam C., Lango Allen, Hana, Bradley, Lisa, Brady, Angela F., Carley, Helena, Carmichael, Jenny, Castle, Bruce, Cilliers, Deirdre, Cox, Helen, Deshpande, Charu, Dixit, Abhijit, Eason, Jacqueline, Elmslie, Frances, Fry, Andrew E., Fryer, Alan, Holder, Muriel, Homfray, Tessa, Kivuva, Emma, McKay, Victoria, Newbury‐Ecob, Ruth, Parker, Michael, Savarirayan, Ravi, Searle, Claire, Shannon, Nora, Shears, Deborah, Smithson, Sarah, Thomas, Ellen, Turnpenny, Peter D., Varghese, Vinod, Vasudevan, Pradeep, Wakeling, Emma, Baple, Emma L., Ellard, Sian
Publicado 2017

De Novo Missense Substitutions in the Gene Encoding CDK8, a Regulator of the Mediator Complex, Cause a Syndromic Developmental Disorder

por Calpena, Eduardo, Hervieu, Alexia, Kaserer, Teresa, Swagemakers, Sigrid M.A., Goos, Jacqueline A.C., Popoola, Olajumoke, Ortiz-Ruiz, Maria Jesus, Barbaro-Dieber, Tina, Bownass, Lucy, Brilstra, Eva H., Brimble, Elise, Foulds, Nicola, Grebe, Theresa A., Harder, Aster V.E., Lees, Melissa M., Monaghan, Kristin G., Newbury-Ecob, Ruth A., Ong, Kai-Ren, Osio, Deborah, Reynoso Santos, Francis Jeshira, Ruzhnikov, Maura R.Z., Telegrafi, Aida, van Binsbergen, Ellen, van Dooren, Marieke F., van der Spek, Peter J., Blagg, Julian, Twigg, Stephen R.F., Mathijssen, Irene M.J., Clarke, Paul A., Wilkie, Andrew O.M.
Publicado 2019

Comprehensive study of 28 individuals with SIN3A-related disorder underscoring the associated mild cognitive and distinctive facial phenotype

por Balasubramanian, Meena, Dingemans, Alexander J. M., Albaba, Shadi, Richardson, Ruth, Yates, Thabo M., Cox, Helen, Douzgou, Sofia, Armstrong, Ruth, Sansbury, Francis H., Burke, Katherine B., Fry, Andrew E., Ragge, Nicola, Sharif, Saba, Foster, Alison, De Sandre-Giovannoli, Annachiara, Elouej, Sahar, Vasudevan, Pradeep, Mansour, Sahar, Wilson, Kate, Stewart, Helen, Heide, Solveig, Nava, Caroline, Keren, Boris, Demirdas, Serwet, Brooks, Alice S., Vincent, Marie, Isidor, Bertrand, Küry, Sebastien, Schouten, Meyke, Leenders, Erika, Chung, Wendy K., Haeringen, Arie van, Scheffner, Thomas, Debray, Francois-Guillaume, White, Susan M., Palafoll, Maria Irene Valenzuela, Pfundt, Rolph, Newbury-Ecob, Ruth, Kleefstra, Tjitske
Publicado 2021

Longitudinal Lung Function Assessment of Patients Hospitalized With COVID-19 Using (1)H and (129)Xe Lung MRI

por Saunders, Laura C., Collier, Guilhem J., Chan, Ho-Fung, Hughes, Paul J.C., Smith, Laurie J., Watson, James, Meiring, James, Gabriel, Zoë, Newman, Thomas, Plowright, Megan, Wade, Phillip, Eaden, James A., Thomas, S., Strickland, S., Gustafsson, L., Bray, Jody, Marshall, Helen, Capener, David J., Armstrong, Leanne, Rodgers, Jennifer, Brook, Martin, Biancardi, Alberto M., Rao, Madhwesha R., Norquay, Graham, Rodgers, Oliver, Munro, Ryan, Ball, James E., Stewart, Neil J., Lawrie, Allan, Jenkins, Gisli, Grist, James, Gleeson, Fergus, Schulte, Rolf F., Johnson, Kevin M., Wilson, Frederick J., Cahn, Anthony, Swift, Andrew J., Rajaram, Smitha, Mills, Gary H., Watson, Lisa, Collini, Paul J., Lawson, Rod, Thompson, A.A. Roger, Wild, Jim M.
Publicado 2023

The Tatton-Brown-Rahman Syndrome: A clinical study of 55 individuals with de novo constitutive DNMT3A variants

por Tatton-Brown, Katrina, Zachariou, Anna, Loveday, Chey, Renwick, Anthony, Mahamdallie, Shazia, Aksglaede, Lise, Baralle, Diana, Barge-Schaapveld, Daniela, Blyth, Moira, Bouma, Mieke, Breckpot, Jeroen, Crabb, Beau, Dabir, Tabib, Cormier-Daire, Valerie, Fauth, Christine, Fisher, Richard, Gener, Blanca, Goudie, David, Homfray, Tessa, Hunter, Matthew, Jorgensen, Agnete, Kant, Sarina G., Kirally-Borri, Cathy, Koolen, David, Kumar, Ajith, Labilloy, Anatalia, Lees, Melissa, Marcelis, Carlo, Mercer, Catherine, Mignot, Cyril, Miller, Kathryn, Neas, Katherine, Newbury-Ecob, Ruth, Pilz, Daniela T., Posmyk, Renata, Prada, Carlos, Ramsey, Keri, Randolph, Linda M., Selicorni, Angelo, Shears, Deborah, Suri, Mohnish, Temple, I. Karen, Turnpenny, Peter, Van Maldergem, Lionel, Varghese, Vinod, Veenstra-Knol, Hermine E., Yachelevich, Naomi, Yates, Laura, Rahman, Nazneen
Publicado 2018

Prenatal exome sequencing analysis in fetal structural anomalies detected by ultrasonography (PAGE): a cohort study

por Lord, Jenny, McMullan, Dominic J, Eberhardt, Ruth Y, Rinck, Gabriele, Hamilton, Susan J, Quinlan-Jones, Elizabeth, Prigmore, Elena, Keelagher, Rebecca, Best, Sunayna K, Carey, Georgina K, Mellis, Rhiannon, Robart, Sarah, Berry, Ian R, Chandler, Kate E, Cilliers, Deirdre, Cresswell, Lara, Edwards, Sandra L, Gardiner, Carol, Henderson, Alex, Holden, Simon T, Homfray, Tessa, Lester, Tracy, Lewis, Rebecca A, Newbury-Ecob, Ruth, Prescott, Katrina, Quarrell, Oliver W, Ramsden, Simon C, Roberts, Eileen, Tapon, Dagmar, Tooley, Madeleine J, Vasudevan, Pradeep C, Weber, Astrid P, Wellesley, Diana G, Westwood, Paul, White, Helen, Parker, Michael, Williams, Denise, Jenkins, Lucy, Scott, Richard H, Kilby, Mark D, Chitty, Lyn S, Hurles, Matthew E, Maher, Eamonn R
Publicado 2019

Further delineation of the KAT6B molecular and phenotypic spectrum

por Gannon, Tamsin, Perveen, Rahat, Schlecht, Hélene, Ramsden, Simon, Anderson, Beverley, Kerr, Bronwyn, Day, Ruth, Banka, Siddharth, Suri, Mohnish, Berland, Siren, Gabbett, Michael, Ma, Alan, Lyonnet, Stan, Cormier-Daire, Valerie, Yilmaz, Rüstem, Borck, Guntram, Wieczorek, Dagmar, Anderlid, Britt-Marie, Smithson, Sarah, Vogt, Julie, Moore-Barton, Heather, Simsek-Kiper, Pelin Ozlem, Maystadt, Isabelle, Destrée, Anne, Bucher, Jessica, Angle, Brad, Mohammed, Shehla, Wakeling, Emma, Price, Sue, Singer, Amihood, Sznajer, Yves, Toutain, Annick, Haye, Damien, Newbury-Ecob, Ruth, Fradin, Melanie, McGaughran, Julie, Tuysuz, Beyhan, Tein, Mark, Bouman, Katelijne, Dabir, Tabib, Van den Ende, Jenneke, Luk, Ho Ming, Pilz, Daniela T, Eason, Jacqueline, Davies, Sally, Reardon, Willie, Garavelli, Livia, Zuffardi, Orsetta, Devriendt, Koen, Armstrong, Ruth, Johnson, Diana, Doco-Fenzy, Martine, Bijlsma, Emilia, Unger, Sheila, Veenstra-Knol, Hermine E, Kohlhase, Jürgen, Lo, Ivan FM, Smith, Janine, Clayton-Smith, Jill
Publicado 2015

Genetic Analysis of ‘PAX6-Negative’ Individuals with Aniridia or Gillespie Syndrome

por Ansari, Morad, Rainger, Jacqueline, Hanson, Isabel M., Williamson, Kathleen A., Sharkey, Freddie, Harewood, Louise, Sandilands, Angela, Clayton-Smith, Jill, Dollfus, Helene, Bitoun, Pierre, Meire, Francoise, Fantes, Judy, Franco, Brunella, Lorenz, Birgit, Taylor, David S., Stewart, Fiona, Willoughby, Colin E., McEntagart, Meriel, Khaw, Peng Tee, Clericuzio, Carol, Van Maldergem, Lionel, Williams, Denise, Newbury-Ecob, Ruth, Traboulsi, Elias I., Silva, Eduardo D., Madlom, Mukhlis M., Goudie, David R., Fleck, Brian W., Wieczorek, Dagmar, Kohlhase, Juergen, McTrusty, Alice D., Gardiner, Carol, Yale, Christopher, Moore, Anthony T., Russell-Eggitt, Isabelle, Islam, Lily, Lees, Melissa, Beales, Philip L., Tuft, Stephen J., Solano, Juan B., Splitt, Miranda, Hertz, Jens Michael, Prescott, Trine E., Shears, Deborah J., Nischal, Ken K., Doco-Fenzy, Martine, Prieur, Fabienne, Temple, I. Karen, Lachlan, Katherine L., Damante, Giuseppe, Morrison, Danny A., van Heyningen, Veronica, FitzPatrick, David R.
Publicado 2016

Distinct genetic architectures for syndromic and nonsyndromic congenital heart defects identified by exome sequencing

por Sifrim, Alejandro, Hitz, Marc-Phillip, Wilsdon, Anna, Breckpot, Jeroen, Al Turki, Saeed H., Thienpont, Bernard, McRae, Jeremy, Fitzgerald, Tomas W, Singh, Tarjinder, Swaminathan, Ganesh Jawahar, Prigmore, Elena, Rajan, Diana, Abdul-Khaliq, Hashim, Banka, Siddharth, Bauer, Ulrike M. M., Bentham, Jamie, Berger, Felix, Bhattacharya, Shoumo, Bu'Lock, Frances, Canham, Natalie, Colgiu, Irina-Gabriela, Cosgrove, Catherine, Cox, Helen, Daehnert, Ingo, Daly, Allan, Danesh, John, Fryer, Alan, Gewillig, Marc, Hobson, Emma, Hoff, Kirstin, Homfray, Tessa, Kahlert, Anne-Karin, Ketley, Ami, Kramer, Hans-Heiner, Lachlan, Katherine, Lampe, Anne Katrin, Louw, Jacoba J., Manickara, Ashok Kumar, Manase, Dorin, McCarthy, Karen P., Metcalfe, Kay, Moore, Carmel, Newbury-Ecob, Ruth, Omer, Seham Osman, Ouwehand, Willem H., Park, Soo-Mi, Parker, Michael J., Pickardt, Thomas, Pollard, Martin O., Robert, Leema, Roberts, David J., Sambrook, Jennifer, Setchfield, Kerry, Stiller, Brigitte, Thornborough, Chris, Toka, Okan, Watkins, Hugh, Williams, Denise, Wright, Michael, Mital, Seema, Daubeney, Piers E. F., Keavney, Bernard, Goodship, Judith, Abu-Sulaiman, Riyadh Mahdi, Klaassen, Sabine, Wright, Caroline F., Firth, Helen V., Barrett, Jeffrey C., Devriendt, Koenraad, FitzPatrick, David R., Brook, J. David, Hurles, Matthew
Publicado 2016

CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language

por Snijders Blok, Lot, Rousseau, Justine, Twist, Joanna, Ehresmann, Sophie, Takaku, Motoki, Venselaar, Hanka, Rodan, Lance H., Nowak, Catherine B., Douglas, Jessica, Swoboda, Kathryn J., Steeves, Marcie A., Sahai, Inderneel, Stumpel, Connie T. R. M., Stegmann, Alexander P. A., Wheeler, Patricia, Willing, Marcia, Fiala, Elise, Kochhar, Aaina, Gibson, William T., Cohen, Ana S. A., Agbahovbe, Ruky, Innes, A. Micheil, Au, P. Y. Billie, Rankin, Julia, Anderson, Ilse J., Skinner, Steven A., Louie, Raymond J., Warren, Hannah E., Afenjar, Alexandra, Keren, Boris, Nava, Caroline, Buratti, Julien, Isapof, Arnaud, Rodriguez, Diana, Lewandowski, Raymond, Propst, Jennifer, van Essen, Ton, Choi, Murim, Lee, Sangmoon, Chae, Jong H., Price, Susan, Schnur, Rhonda E., Douglas, Ganka, Wentzensen, Ingrid M., Zweier, Christiane, Reis, André, Bialer, Martin G., Moore, Christine, Koopmans, Marije, Brilstra, Eva H., Monroe, Glen R., van Gassen, Koen L. I., van Binsbergen, Ellen, Newbury-Ecob, Ruth, Bownass, Lucy, Bader, Ingrid, Mayr, Johannes A., Wortmann, Saskia B., Jakielski, Kathy J., Strand, Edythe A., Kloth, Katja, Bierhals, Tatjana, Roberts, John D., Petrovich, Robert M., Machida, Shinichi, Kurumizaka, Hitoshi, Lelieveld, Stefan, Pfundt, Rolph, Jansen, Sandra, Deriziotis, Pelagia, Faivre, Laurence, Thevenon, Julien, Assoum, Mirna, Shriberg, Lawrence, Kleefstra, Tjitske, Brunner, Han G., Wade, Paul A., Fisher, Simon E., Campeau, Philippe M.
Publicado 2018

Author Correction: CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language

por Blok, Lot Snijders, Rousseau, Justine, Twist, Joanna, Ehresmann, Sophie, Takaku, Motoki, Venselaar, Hanka, Rodan, Lance H., Nowak, Catherine B., Douglas, Jessica, Swoboda, Kathryn J., Steeves, Marcie A., Sahai, Inderneel, Stumpel, Connie T. R. M., Stegmann, Alexander P. A., Wheeler, Patricia, Willing, Marcia, Fiala, Elise, Kochhar, Aaina, Gibson, William T., Cohen, Ana S. A., Agbahovbe, Ruky, Innes, A. Micheil, Au, P. Y. Billie, Rankin, Julia, Anderson, Ilse J., Skinner, Steven A., Louie, Raymond J., Warren, Hannah E., Afenjar, Alexandra, Keren, Boris, Nava, Caroline, Buratti, Julien, Isapof, Arnaud, Rodriguez, Diana, Lewandowski, Raymond, Propst, Jennifer, van Essen, Ton, Choi, Murim, Lee, Sangmoon, Chae, Jong H., Price, Susan, Schnur, Rhonda E., Douglas, Ganka, Wentzensen, Ingrid M., Zweier, Christiane, Reis, André, Bialer, Martin G., Moore, Christine, Koopmans, Marije, Brilstra, Eva H., Monroe, Glen R., van Gassen, Koen L. I., van Binsbergen, Ellen, Newbury-Ecob, Ruth, Bownass, Lucy, Bader, Ingrid, Mayr, Johannes A., Wortmann, Saskia B., Jakielski, Kathy J., Strand, Edythe A., Kloth, Katja, Bierhals, Tatjana, Roberts, John D., Petrovich, Robert M., Machida, Shinichi, Kurumizaka, Hitoshi, Lelieveld, Stefan, Pfundt, Rolph, Jansen, Sandra, Deriziotis, Pelagia, Faivre, Laurence, Thevenon, Julien, Assoum, Mirna, Shriberg, Lawrence, Kleefstra, Tjitske, Brunner, Han G., Wade, Paul A., Fisher, Simon E., Campeau, Philippe M.
Publicado 2019

Author Correction: CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language

por Snijders Blok, Lot, Rousseau, Justine, Twist, Joanna, Ehresmann, Sophie, Takaku, Motoki, Venselaar, Hanka, Rodan, Lance H., Nowak, Catherine B., Douglas, Jessica, Swoboda, Kathryn J., Steeves, Marcie A., Sahai, Inderneel, Stumpel, Connie T. R. M., Stegmann, Alexander P. A., Wheeler, Patricia, Willing, Marcia, Fiala, Elise, Kochhar, Aaina, Gibson, William T., Cohen, Ana S. A., Agbahovbe, Ruky, Innes, A. Micheil, Au, P. Y. Billie, Rankin, Julia, Anderson, Ilse J., Skinner, Steven A., Louie, Raymond J., Warren, Hannah E., Afenjar, Alexandra, Keren, Boris, Nava, Caroline, Buratti, Julien, Isapof, Arnaud, Rodriguez, Diana, Lewandowski, Raymond, Propst, Jennifer, van Essen, Ton, Choi, Murim, Lee, Sangmoon, Chae, Jong H., Price, Susan, Schnur, Rhonda E., Douglas, Ganka, Wentzensen, Ingrid M., Zweier, Christiane, Reis, André, Bialer, Martin G., Moore, Christine, Koopmans, Marije, Brilstra, Eva H., Monroe, Glen R., van Gassen, Koen L. I., van Binsbergen, Ellen, Newbury-Ecob, Ruth, Bownass, Lucy, Bader, Ingrid, Mayr, Johannes A., Wortmann, Saskia B., Jakielski, Kathy J., Strand, Edythe A., Kloth, Katja, Bierhals, Tatjana, Roberts, John D., Petrovich, Robert M., Machida, Shinichi, Kurumizaka, Hitoshi, Lelieveld, Stefan, Pfundt, Rolph, Jansen, Sandra, Deriziotis, Pelagia, Faivre, Laurence, Thevenon, Julien, Assoum, Mirna, Shriberg, Lawrence, Kleefstra, Tjitske, Brunner, Han G., Wade, Paul A., Fisher, Simon E., Campeau, Philippe M.
Publicado 2019

Effects of COVID-19 Pandemic on Voluntary Medical Male Circumcision Services for HIV Prevention, Sub-Saharan Africa, 2020

por Peck, Megan E., Ong, Katherine S., Lucas, Todd, Prainito, Amber, Thomas, Anne G., Brun, Alex, Kiggundu, Valerian, Yansaneh, Aisha, Busang, Lesego, Kgongwana, Kabelo, Kelaphile, David, Seipone, Khumo, Letebele, Mpho H., Makadzange, Panganai F., Marwiro, Amon, Sesinyi, Mirriam, Lapidos, Tyrone, Lukhele, Njabuliso, Maziya, Vusi, Mkhontfo, Mandzisi, Gultie, Teruwork, Mulatu, Dejene, Shimelis, Mesfin, Zegeye, Tiruneh, Teka, Tesfaye, Bulterys, Marc, Njenga, John N., Odoyo-June, Elijah, Juma, Ambrose W., Soo, Leonard, Talam, Norah, Brown, Malerato, Chakare, Tafadzwa, Nonyana, Nyane, Khoabane, Mpho A., Auld, Andrew F., Maida, Alice, Msungama, Wezi, Kapito, Martin, Nyirenda, Rose, Matchere, Faustin, Odek, James, Canda, Marcos, Malimane, Inácio, Come, Jotamo, Gaspar, Nuno, Langa, Antonio, Aupokolo, Mekondjo A., Vejorerako, Kaauma C., Kahindi, Lawrence, Mali, Denis, Zegeye, Abeje, Mangoya, Derek, Zemburuka, Brigitte L., Bamwesigye, Jackson, Kankindi, Ida, Kayirangwa, Eugenie, Malamba, Samuel S., Roels, Thierry, Kayonde, Lenny, Zimulinda, Eugene, Ndengo, Emah, Nsanzimana, Sabin, Remera, Eric, Rwibasira, Gallican N., Sangwayire, Beata, Semakula, Muhammed, Rugira, Eugene, Rugwizangoga, Eugene, Tubane, Emmanuel, Yoboka, Emmanuel, Lawrence, Joseph, Loykissoonlal, Dayanund, Maphothi, Nandi, Achut, Victoria, Bunga, Sudhir, Moi, Monday, Amuri, Mbaraka, Kazaura, Kokuhumbya, Simbeye, Daimon, Fida, Neway, Kayange, Alick A., Seleman, Mohamed, Akao, Juliet, Alamo, Stella T., Kabuye, Geoffrey, Kyobutungi, Sheila, Makumbi, Fredrick E., Mudiope, Peter, Nantez, Barbara, Chituwo, Omega, Godfrey, Lingenda, Muyunda, Brian, Kamboyi, Royd, Masiye, Joseph, Lifuka, Eda, Mandisarisa, John, Mhangara, Mutsa, Xaba, Sinokuthemba, Toledo, Carlos
Publicado 2022

Genome-wide analyses of individual differences in quantitatively assessed reading- and language-related skills in up to 34,000 people

por Eising, Else, Mirza-Schreiber, Nazanin, de Zeeuw, Eveline L., Wang, Carol A., Truong, Dongnhu T., Allegrini, Andrea G., Shapland, Chin Yang, Zhu, Gu, Wigg, Karen G., Gerritse, Margot L., Molz, Barbara, Alagöz, Gökberk, Gialluisi, Alessandro, Abbondanza, Filippo, Rimfeld, Kaili, van Donkelaar, Marjolein, Liao, Zhijie, Jansen, Philip R., Andlauer, Till F. M., Bates, Timothy C., Bernard, Manon, Blokland, Kirsten, Bonte, Milene, Børglum, Anders D., Bourgeron, Thomas, Brandeis, Daniel, Ceroni, Fabiola, Csépe, Valéria, Dale, Philip S., de Jong, Peter F., DeFries, John C., Démonet, Jean-François, Demontis, Ditte, Feng, Yu, Gordon, Scott D., Guger, Sharon L., Hayiou-Thomas, Marianna E., Hernández-Cabrera, Juan A., Hottenga, Jouke-Jan, Hulme, Charles, Kere, Juha, Kerr, Elizabeth N., Koomar, Tanner, Landerl, Karin, Leonard, Gabriel T., Lovett, Maureen W., Lyytinen, Heikki, Martin, Nicholas G., Martinelli, Angela, Maurer, Urs, Michaelson, Jacob J., Moll, Kristina, Monaco, Anthony P., Morgan, Angela T., Nöthen, Markus M., Pausova, Zdenka, Pennell, Craig E., Pennington, Bruce F., Price, Kaitlyn M., Rajagopal, Veera M., Ramus, Franck, Richer, Louis, Simpson, Nuala H., Smith, Shelley D., Snowling, Margaret J., Stein, John, Strug, Lisa J., Talcott, Joel B., Tiemeier, Henning, van der Schroeff, Marc P., Verhoef, Ellen, Watkins, Kate E., Wilkinson, Margaret, Wright, Margaret J., Barr, Cathy L., Boomsma, Dorret I., Carreiras, Manuel, Franken, Marie-Christine J., Gruen, Jeffrey R., Luciano, Michelle, Müller-Myhsok, Bertram, Newbury, Dianne F., Olson, Richard K., Paracchini, Silvia, Paus, Tomáš, Plomin, Robert, Reilly, Sheena, Schulte-Körne, Gerd, Tomblin, J. Bruce, van Bergen, Elsje, Whitehouse, Andrew J. O., Willcutt, Erik G., St Pourcain, Beate, Francks, Clyde, Fisher, Simon E.
Publicado 2022

Large-scale discovery of novel genetic causes of developmental disorders

por Fitzgerald, TW, Gerety, SS, Jones, WD, van Kogelenberg, M, King, DA, McRae, J, Morley, KI, Parthiban, V, Al-Turki, S, Ambridge, K, Barrett, DM, Bayzetinova, T, Clayton, S, Coomber, EL, Gribble, S, Jones, P, Krishnappa, N, Mason, LE, Middleton, A, Miller, R, Prigmore, E, Rajan, D, Sifrim, A, Tivey, AR, Ahmed, M, Akawi, N, Andrews, R, Anjum, U, Archer, H, Armstrong, R, Balasubramanian, M, Banerjee, R, Baralle, D, Batstone, P, Baty, D, Bennett, C, Berg, J, Bernhard, B, Bevan, AP, Blair, E, Blyth, M, Bohanna, D, Bourdon, L, Bourn, D, Brady, A, Bragin, E, Brewer, C, Brueton, L, Brunstrom, K, Bumpstead, SJ, Bunyan, DJ, Burn, J, Burton, J, Canham, N, Castle, B, Chandler, K, Clasper, S, Clayton-Smith, J, Cole, T, Collins, A, Collinson, MN, Connell, F, Cooper, N, Cox, H, Cresswell, L, Cross, G, Crow, Y, D’Alessandro, M, Dabir, T, Davidson, R, Davies, S, Dean, J, Deshpande, C, Devlin, G, Dixit, A, Dominiczak, A, Donnelly, C, Donnelly, D, Douglas, A, Duncan, A, Eason, J, Edkins, S, Ellard, S, Ellis, P, Elmslie, F, Evans, K, Everest, S, Fendick, T, Fisher, R, Flinter, F, Foulds, N, Fryer, A, Fu, B, Gardiner, C, Gaunt, L, Ghali, N, Gibbons, R, Gomes Pereira, SL, Goodship, J, Goudie, D, Gray, E, Greene, P, Greenhalgh, L, Harrison, L, Hawkins, R, Hellens, S, Henderson, A, Hobson, E, Holden, S, Holder, S, Hollingsworth, G, Homfray, T, Humphreys, M, Hurst, J, Ingram, S, Irving, M, Jarvis, J, Jenkins, L, Johnson, D, Jones, D, Jones, E, Josifova, D, Joss, S, Kaemba, B, Kazembe, S, Kerr, B, Kini, U, Kinning, E, Kirby, G, Kirk, C, Kivuva, E, Kraus, A, Kumar, D, Lachlan, K, Lam, W, Lampe, A, Langman, C, Lees, M, Lim, D, Lowther, G, Lynch, SA, Magee, A, Maher, E, Mansour, S, Marks, K, Martin, K, Maye, U, McCann, E, McConnell, V, McEntagart, M, McGowan, R, McKay, K, McKee, S, McMullan, DJ, McNerlan, S, Mehta, S, Metcalfe, K, Miles, E, Mohammed, S, Montgomery, T, Moore, D, Morgan, S, Morris, A, Morton, J, Mugalaasi, H, Murday, V, Nevitt, L, Newbury-Ecob, R, Norman, A, O'Shea, R, Ogilvie, C, Park, S, Parker, MJ, Patel, C, Paterson, J, Payne, S, Phipps, J, Pilz, DT, Porteous, D, Pratt, N, Prescott, K, Price, S, Pridham, A, Procter, A, Purnell, H, Ragge, N, Rankin, J, Raymond, L, Rice, D, Robert, L, Roberts, E, Roberts, G, Roberts, J, Roberts, P, Ross, A, Rosser, E, Saggar, A, Samant, S, Sandford, R, Sarkar, A, Schweiger, S, Scott, C, Scott, R, Selby, A, Seller, A, Sequeira, C, Shannon, N, Sharif, S, Shaw-Smith, C, Shearing, E, Shears, D, Simonic, I, Simpkin, D, Singzon, R, Skitt, Z, Smith, A, Smith, B, Smith, K, Smithson, S, Sneddon, L, Splitt, M, Squires, M, Stewart, F, Stewart, H, Suri, M, Sutton, V, Swaminathan, GJ, Sweeney, E, Tatton-Brown, K, Taylor, C, Taylor, R, Tein, M, Temple, IK, Thomson, J, Tolmie, J, Torokwa, A, Treacy, B, Turner, C, Turnpenny, P, Tysoe, C, Vandersteen, A, Vasudevan, P, Vogt, J, Wakeling, E, Walker, D, Waters, J, Weber, A, Wellesley, D, Whiteford, M, Widaa, S, Wilcox, S, Williams, D, Williams, N, Woods, G, Wragg, C, Wright, M, Yang, F, Yau, M, Carter, NP, Parker, M, Firth, HV, FitzPatrick, DR, Wright, CF, Barrett, JC, Hurles, ME
Publicado 2014

Proceedings of the 14th annual conference of INEBRIA: New York, NY, USA, September 14–15, 2017

por Holloway, Aisha S., Ferguson, Jennifer, Landale, Sarah, Cariola, Laura, Newbury-Birch, Dorothy, Flynn, Amy, Knight, John R., Sherritt, Lon, Harris, Sion K., O’Donnell, Amy J., Kaner, Eileen, Hanratty, Barbara, Loree, Amy M., Yonkers, Kimberly A., Ondersma, Steven J., Gilstead-Hayden, Kate, Martino, Steve, Adam, Angeline, Schwartz, Robert P., Wu, Li-Tzy, Subramaniam, Geetha, Sharma, Gaurav, McNeely, Jennifer, Berman, Anne H., Kolaas, Karoline, Petersén, Elisabeth, Bendtsen, Preben, Hedman, Erik, Linderoth, Catharina, Müssener, Ulrika, Sinadinovic, Kristina, Spak, Fredrik, Gremyr, Ida, Thurang, Anna, Mitchell, Ann M., Finnell, Deborah, Savage, Christine L., Mahmoud, Khadejah F., Riordan, Benjamin C., Conner, Tamlin S., Flett, Jayde A. M., Scarf, Damian, McRee, Bonnie, Vendetti, Janice, Gallucci, Karen Steinberg, Robaina, Kate, Clark, Brendan J., Jones, Jacqueline, Reed, Kathryne D., Hodapp, Rachel M., Douglas, Ivor, Burnham, Ellen L., Aagaard, Laura, Cook, Paul F., Harris, Brett R., Yu, Jiang, Wolff, Margaret, Rogers, Meighan, Barbosa, Carolina, Wedehase, Brendan J., Dunlap, Laura J., Mitchell, Shannon G., Dusek, Kristi A., Gryczynski, Jan, Kirk, Arethusa S., Oros, Marla T., Hosler, Colleen, O’Grady, Kevin E., Brown, Barry S., Angus, Colin, Sherborne, Sidney, Gillespie, Duncan, Meier, Petra, Brennan, Alan, de Vargas, Divane, Soares, Janaina, Castelblanco, Donna, Doran, Kelly M., Wittman, Ian, Shelley, Donna, Rotrosen, John, Gelberg, Lillian, Edelman, E. Jennifer, Maisto, Stephen A., Hansen, Nathan B., Cutter, Christopher J., Deng, Yanhong, Dziura, James, Fiellin, Lynn E., O’Connor, Patrick G., Bedimo, Roger, Gibert, Cynthia, Marconi, Vincent C., Rimland, David, Rodriguez-Barradas, Maria C., Simberkoff, Michael S., Justice, Amy C., Bryant, Kendall J., Fiellin, David A., Giles, Emma L., Coulton, Simon, Deluca, Paolo, Drummond, Colin, Howel, Denise, McColl, Elaine, McGovern, Ruth, Scott, Stephanie, Stamp, Elaine, Sumnall, Harry, Vale, Luke, Alabani, Viviana, Atkinson, Amanda, Boniface, Sadie, Frankham, Jo, Gilvarry, Eilish, Hendrie, Nadine, Howe, Nicola, McGeechan, Grant J., Ramsey, Amy, Stanley, Grant, Clephane, Justine, Gardiner, David, Holmes, John, Martin, Neil, Shevills, Colin, Soutar, Melanie, Chi, Felicia W., Weisner, Constance, Ross, Thekla B., Mertens, Jennifer, Sterling, Stacy A., Shorter, Gillian W., Heather, Nick, Bray, Jeremy, Cohen, Hildie A., McPherson, Tracy L., Adam, Cyrille, López-Pelayo, Hugo, Gual, Antoni, Segura-Garcia, Lidia, Colom, Joan, Ornelas, India J., Doyle, Suzanne, Donovan, Dennis, Duran, Bonnie, Torres, Vanessa, Gaume, Jacques, Grazioli, Véronique, Fortini, Cristiana, Paroz, Sophie, Bertholet, Nicolas, Daeppen, Jean-Bernard, Satterfield, Jason M., Gregorich, Steven, Alvarado, Nicholas J., Muñoz, Ricardo, Kulieva, Gozel, Vijayaraghavan, Maya, Adam, Angéline, Cunningham, John A., Díaz, Estela, Palacio-Vieira, Jorge, Godinho, Alexandra, Kushir, Vladyslav, O’Brien, Kimberly H. M., Aguinaldo, Laika D., Sellers, Christina M., Spirito, Anthony, Chang, Grace, Blake-Lamb, Tiffany, LaFave, Lea R. Ayers, Thies, Kathleen M., Pepin, Amy L., Sprangers, Kara E., Bradley, Martha, Jorgensen, Shasta, Catano, Nico A., Murray, Adelaide R., Schachter, Deborah, Andersen, Ronald M., Rey, Guillermina Natera, Vahidi, Mani, Rico, Melvin W., Baumeister, Sebastian E., Johansson, Magnus, Sinadinovic, Christina, Hermansson, Ulric, Andreasson, Sven, O’Grady, Megan A., Kapoor, Sandeep, Akkari, Cherine, Bernal, Camila, Pappacena, Kristen, Morley, Jeanne, Auerbach, Mark, Neighbors, Charles J., Kwon, Nancy, Conigliaro, Joseph, Morgenstern, Jon, Magill, Molly, Apodaca, Timothy R., Borsari, Brian, Hoadley, Ariel, Scott Tonigan, J., Moyers, Theresa, Fitzgerald, Niamh M., Schölin, Lisa, Barticevic, Nicolas, Zuzulich, Soledad, Poblete, Fernando, Norambuena, Pablo, Sacco, Paul, Ting, Laura, Beaulieu, Michele, Wallace, Paul George, Andrews, Matthew, Daley, Kate, Shenker, Don, Gallagher, Louise, Watson, Rod, Weaver, Tim, Bruguera, Pol, Oliveras, Clara, Gavotti, Carolina, Barrio, Pablo, Braddick, Fleur, Miquel, Laia, Suárez, Montse, Bruguera, Carla, Brown, Richard L., Capell, Julie Whelan, Paul Moberg, D., Maslowsky, Julie, Saunders, Laura A., McCormack, Ryan P., Scheidell, Joy, Gonzalez, Mirelis, Bauroth, Sabrina, Liu, Weiwei, Lindsay, Dawn L., Lincoln, Piper, Hagle, Holly, Wallhed Finn, Sara, Hammarberg, Anders, Andréasson, Sven, King, Sarah E., Vargo, Rachael, Kameg, Brayden N., Acquavita, Shauna P., Van Loon, Ruth Anne, Smith, Rachel, Brehm, Bonnie J., Diers, Tiffiny, Kim, Karissa, Barker, Andrea, Jones, Ashley L., Skinner, Asheley C., Hinman, Agatha, Svikis, Dace S., Thacker, Casey L., Resnicow, Ken, Beatty, Jessica R., Janisse, James, Puder, Karoline, Bakshi, Ann-Sofie, Milward, Joanna M., Kimergard, Andreas, Garnett, Claire V., Crane, David, Brown, Jamie, West, Robert, Michie, Susan, Rosendahl, Ingvar, Andersson, Claes, Gajecki, Mikael, Blankers, Matthijs, Donoghue, Kim, Lynch, Ellen, Maconochie, Ian, Phillips, Ceri, Pockett, Rhys, Phillips, Tom, Patton, R., Russell, Ian, Strang, John, Stewart, Maureen T., Quinn, Amity E., Brolin, Mary, Evans, Brooke, Horgan, Constance M., Liu, Junqing, McCree, Fern, Kanovsky, Doug, Oberlander, Tyler, Zhang, Huan, Hamlin, Ben, Saunders, Robert, Barton, Mary B., Scholle, Sarah H., Santora, Patricia, Bhatt, Chirag, Ahmed, Kazi, Hodgkin, Dominic, Gao, Wenwu, Merrick, Elizabeth L., Drebing, Charles E., Larson, Mary Jo, Sharma, Monica, Petry, Nancy M., Saitz, Richard, Weisner, Constance M., Young-Wolff, Kelly C., Lu, Wendy Y., Blosnich, John R., Lehavot, Keren, Glass, Joseph E., Williams, Emily C., Bensley, Kara M., Chan, Gary, Dombrowski, Julie, Fortney, John, Rubinsky, Anna D., Lapham, Gwen T., Forray, Ariadna, Olmstead, Todd A., Gilstad-Hayden, Kathryn, Kershaw, Trace, Dillon, Pamela, Weaver, Michael F., Grekin, Emily R., Ellis, Jennifer D., McGoron, Lucy, McGoron, Lucy
Publicado 2017